FAM155A
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Protein-coding gene in the species Homo sapiens
| NALF1 | |||||||||||||||||||||||||||||||||||||||||||||||
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| Aliases | NALF1 , family with sequence similarity 155 member A, NLF-1, NALCN channel auxiliary factor 1, FAM155A | ||||||||||||||||||||||||||||||||||||||||||||||
| External IDs | MGI: 2142765; HomoloGene: 83472; GeneCards: NALF1; OMA:NALF1 - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||
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Family with sequence similarity 155, member A is a protein that in humans is encoded by the FAM155A gene. [5]
References
[edit ]- ^ a b c GRCh38: Ensembl release 89: ENSG00000204442 – Ensembl, May 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000079157 – Ensembl, May 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Entrez Gene: Family with sequence similarity 155, member A" . Retrieved 2013年11月26日.
Further reading
[edit ]- Anney RJ, Lasky-Su J, O'Dúshláine C, Kenny E, Neale BM, Mulligan A, et al. (December 2008). "Conduct disorder and ADHD: evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study". American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics. 147B (8): 1369–1378. doi:10.1002/ajmg.b.30871. PMID 18951430. S2CID 30325260.
- Cross-Disorder Group of the Psychiatric Genomics Consortium (April 2013). "Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis". Lancet. 381 (9875): 1371–1379. doi:10.1016/S0140-6736(12)62129-1. PMC 3714010 . PMID 23453885.
- Wang K, Zhang H, Bloss CS, Duvvuri V, Kaye W, Schork NJ, et al. (September 2011). "A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa". Molecular Psychiatry. 16 (9): 949–959. doi:10.1038/mp.2010.107. PMC 3859494 . PMID 21079607.
- Li SH, McInnis MG, Margolis RL, Antonarakis SE, Ross CA (June 1993). "Novel triplet repeat containing genes in human brain: cloning, expression, and length polymorphisms". Genomics. 16 (3): 572–579. doi:10.1006/geno.1993.1232 . PMID 8325628.
- Terracciano A, Tanaka T, Sutin AR, Sanna S, Deiana B, Lai S, et al. (November 2010). "Genome-wide association scan of trait depression". Biological Psychiatry. 68 (9): 811–817. doi:10.1016/j.biopsych.2010年06月03日0. PMC 2955852 . PMID 20800221.
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